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BRANEMARK SYSTEM-5.0MM FIXTURE

K911961 Class II Traditional
Decision Date
1991-07-25
Sponsor / Applicant
Nobelpharma USA, Inc.

Technical Specification

510(k) Submission ID K911961
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 1991-07-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BRANEMARK SYSTEM-5.0MM FIXTURE received FDA 510(k) clearance under submission number K911961, sponsored by Nobelpharma USA, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1991-07-25.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.